Variant #0001020136 (NC_000011.9:g.19209833A>G, NM_003476.4:c.131T>C (CSRP3))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.19209833A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID CSRP3_000043 See all 9 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs104894205
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-12-27 16:53:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSRP3 NM_003476.4 +?/. - c.131T>C r.(?) p.(Leu44Pro)


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